Clinical Research Associate II
IQVIA · Auckland, New Zealand
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
IQVIA seeks a Clinical Research Associate II to oversee study site operations and ensure regulatory compliance across clinical trials. The role involves site visits, recruitment strategy development, staff training, and financial management for a contract research organization based in Auckland, New Zealand.
What they're looking for
- Bachelor's degree in scientific or healthcare discipline
- Minimum 4 years on-site monitoring experience
- Strong knowledge of GCP and ICH guidelines
- Proficiency in Microsoft Office and relevant clinical trial technology
- Excellent written and verbal communication skills
- Strong organizational and analytical problem-solving abilities
- Full work rights in New Zealand; sponsorship not available
What you'll be doing
- Conduct site visits from study initiation through close-out to ensure compliance and success
- Develop and implement recruitment strategies to enroll study subjects
- Provide training and maintain communication with study sites
- Evaluate site practices and ensure protocol and regulatory adherence
- Monitor study progress including regulatory submissions and data query resolution
Privacy & handoff
This role links to IQVIA's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.